1214-16-0

Usage

Uses

Used in Organic Electronics:
3,6-DIBROMO-9-VINYLCARBAZOLE is used as a key component in the development of organic electronic devices due to its ability to enhance the performance and stability of these devices.
Used in Photovoltaic Devices:
In the photovoltaic industry, 3,6-DIBROMO-9-VINYLCARBAZOLE is utilized as a material in the production of solar cells, contributing to improved efficiency and durability.
Used in Chemical Sensors:
3,6-DIBROMO-9-VINYLCARBAZOLE is employed as a sensitive component in chemical sensors for its capacity to detect specific chemical compounds, enhancing the sensitivity and selectivity of these sensors.
Used in Synthesis of Complex Organic Compounds:
3,6-DIBROMO-9-VINYLCARBAZOLE serves as a building block in the synthesis of complex organic compounds, facilitating the creation of new molecules with diverse applications in various fields.
Used as a Reagent in Chemical Reactions:
In the chemical industry, 3,6-DIBROMO-9-VINYLCARBAZOLE is used as a reagent to catalyze or participate in various chemical reactions, aiding in the production of desired products.

Upstream product

• 1147-67-7 β-chloro-N-ethyl-3,6-dibromocarbazole 
• 108-05-4 vinyl acetate 
• 6825-20-3 3,6-dibromo-9H-carbazole 

Relevant academic research and scientific papers

Iridium-Catalyzed Vinylation of Carbazole Derivatives with Vinyl Acetate

We report a practical method for the synthesis of vinylcarbazoles via iridium-catalyzed vinylation of carbazoles with vinyl acetate as the vinyl source. This simple and efficient reaction using an iridium catalyst provides a convenient method for producing monomers for the synthesis of poly(N-vinylcarbazole)s, which are used in electroluminescent devices.

Synthesis and photophysical properties of two branched carbazole-based polymers

Two branched carbazole-based polymers having arylene- and arylenevinylene-type structure respectively, were synthesized by copper- or palladium-catalyzed self-polycondensation of AB2 carbazole monomers. The self-Ullmann C-N polycondensation of 3,6-diiodocarbazole led to a branched polymer containing about 15 trisubstituted carbazole (at 3,6 and N-positions) nuclei included in the polymer chain. The self-Heck polycondensation of 3,6-diiodo- or 3,6-dibromo-N-vinylcarbazole led to a branched polyarylenevinylene with trisubstituted carbazole nuclei at 3,6 and N-positions. Both polymers were amorphous materials and soluble in organic solvents and their optical and electrochemical properties were comparable with those of similar polymers with linear structure.